Plasticity of hot air-dried mannuronate- and guluronate-rich alginate films

被引:32
作者
Ashikin, Wan Hussin Noor Shimariza [1 ,2 ]
Wong, Tin Wui [1 ,2 ]
Law, Chung Lim [3 ]
机构
[1] Univ Teknol MARA, Fac Pharm, Particle Design Res Grp, Puncak Alam 42300, Selangor, Malaysia
[2] Univ Teknol MARA, Nondestruct Biomed & Pharmaceut Res Ctr, Puncak Alam 42300, Selangor, Malaysia
[3] Univ Nottingham, Sch Chem & Environm Engn, Semenyih 43500, Selangor, Malaysia
关键词
Alginate; Drying; Guluronate; Film; Mannuronate; Plasticity; TRANSDERMAL DRUG-DELIVERY; MOLECULAR-WEIGHT; RELEASE; MICROWAVE;
D O I
10.1016/j.carbpol.2010.02.002
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The plasticity of hot air-dried guluronate-rich (MG) and mannuronate-rich (MC) alginate films prepared from 2% and 4% (w/w) alginate solutions, which contained the same amount of polymer, through hot-air drying at 40-80 degrees C were investigated. These films were subjected to thermomechanical, differential scanning calorimetry, fourier-transform infrared, X-ray diffractometry, dimension, morphology, moisture content, viscosity and polymer molecular weight analysis. Film plasticity increased when dilute alginate solution and MC were employed in film preparation. This was due to decrease in polymer-polymer interaction at high-strength domains of matrix involving C-H, O-H, C-O and/or C=O moiety of alginate, attributing to plasticization effect of water and ease of molecular rearrangement of alginate. The plasticity of film decreased with an increase in drying temperature from 40 to 60 degrees C following heat-induced polymer-polymer interaction. A further increase in drying temperature to 80 degrees C nonetheless greatly promoted film plasticity through air bubble formation and reduced alginate molecular weight in film. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:104 / 113
页数:10
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